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Sandra C. Kirkwood, Ph.D. - Publications

Affiliations: 
2000 Indiana University, Bloomington, Bloomington, IN, United States 
Area:
Genetics
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12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2004 Blekher TM, Yee RD, Kirkwood SC, Hake AM, Stout JC, Weaver MR, Foroud TM. Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington's disease. Vision Research. 44: 2729-36. PMID 15358067 DOI: 10.1016/J.Visres.2004.06.006  0.354
2004 Kaiser S, Foltz LA, George CA, Kirkwood SC, Bemis KG, Lin X, Gelbert LM, Nisenbaum LK. Phencyclidine-induced changes in rat cortical gene expression identified by microarray analysis: implications for schizophrenia. Neurobiology of Disease. 16: 220-35. PMID 15207279 DOI: 10.1016/J.Nbd.2004.01.011  0.336
2003 Pankratz N, Mukhopadhyay N, Huang S, Foroud T, Kirkwood SC. Identification of genes for complex disease using longitudinal phenotypes. Bmc Genetics. 4: S58. PMID 14975126 DOI: 10.1186/1471-2156-4-S1-S58  0.36
2003 O'Donnell BF, Wilt MA, Hake AM, Stout JC, Kirkwood SC, Foroud T. Visual function in Huntington's disease patients and presymptomatic gene carriers. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 1027-34. PMID 14502670 DOI: 10.1002/Mds.10491  0.381
2002 Kirkwood SC, Siemers E, Viken R, Hodes ME, Conneally PM, Christian JC, Foroud T. Longitudinal personality changes among presymptomatic Huntington disease gene carriers. Neuropsychiatry, Neuropsychology, and Behavioral Neurology. 15: 192-7. PMID 12218712  0.544
2001 Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Use of variable marker density, principal components, and neural networks in the dissection of disease etiology Genetic Epidemiology. 21: S732-737. PMID 11793770 DOI: 10.1002/Gepi.2001.21.S1.S732  0.519
2001 McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. Parametric linkage analysis and disequilibrium methods to identify loci for complex disease Genetic Epidemiology. 21: S528-S533. PMID 11793731 DOI: 10.1002/Gepi.2001.21.S1.S528  0.568
2001 Kirkwood SC, Su JL, Conneally PM, Foroud T. Progression of symptoms in the early and middle stages of Huntington disease Archives of Neurology. 58: 273-278. PMID 11176966 DOI: 10.1001/Archneur.58.2.273  0.5
2000 Kirkwood SC, Siemers E, Hodes ME, Conneally PM, Christian JC, Foroud T. Subtle changes among presymptomatic carriers of the Huntington's disease gene. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 773-9. PMID 11080230 DOI: 10.1136/Jnnp.69.6.773  0.595
2000 Kirkwood SC, Siemers E, Bond C, Conneally PM, Christian JC, Foroud T. Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene. Archives of Neurology. 57: 1040-4. PMID 10891987 DOI: 10.1001/Archneur.57.7.1040  0.553
1999 Stoller ML, Bruce JE, Bruce CA, Foroud T, Kirkwood SC, Stambrook PJ. Linkage of type II and type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone- forming phenotype American Journal of Medical Genetics. 86: 134-139. PMID 10449648 DOI: 10.1002/(Sici)1096-8628(19990910)86:2<134::Aid-Ajmg9>3.0.Co;2-H  0.35
1999 Kirkwood SC, Siemers E, Stout JC, Hodes ME, Conneally PM, Christian JC, Foroud T. Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Archives of Neurology. 56: 563-8. PMID 10328251 DOI: 10.1001/Archneur.56.5.563  0.578
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